Division of Gastroenterology, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
Pancreatitis Center, Division of Pancreaticobiliary Surgery, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
Am J Gastroenterol. 2017 Aug;112(8):1320-1329. doi: 10.1038/ajg.2017.106. Epub 2017 Apr 25.
We evaluated factors associated with pathogenic genetic variants in patients with idiopathic pancreatitis.
Genetic testing (PRSS1, CFTR, SPINK1, and CTRC) was performed in all eligible patients with idiopathic pancreatitis between 2010 to 2015. Patients were classified into the following groups based on a review of medical records: (1) acute recurrent idiopathic pancreatitis (ARIP) with or without underlying chronic pancreatitis; (2) idiopathic chronic pancreatitis (ICP) without a history of ARP; (3) an unexplained first episode of acute pancreatitis (AP)<35 years of age; and (4) family history of pancreatitis. Logistic regression analysis was used to determine the factors associated with pathogenic genetic variants.
Among 197 ARIP and/or ICP patients evaluated from 2010 to 2015, 134 underwent genetic testing. A total of 88 pathogenic genetic variants were found in 64 (47.8%) patients. Pathogenic genetic variants were identified in 58, 63, and 27% of patients with ARIP, an unexplained first episode of AP <35 years of age, and ICP without ARP, respectively. ARIP (OR: 18.12; 95% CI: 2.16-151.87; P=0.008) and an unexplained first episode of AP<35 years of age (OR: 2.46; 95% CI: 1.18-5.15; P=0.017), but not ICP, were independently associated with pathogenic genetic variants in the adjusted analysis.
Pathogenic genetic variants are most likely to be identified in patients with ARIP and an unexplained first episode of AP<35 years of age. Genetic testing in these patient populations may delineate an etiology and prevent unnecessary diagnostic testing and procedures.
我们评估了特发性胰腺炎患者与致病性遗传变异相关的因素。
对 2010 年至 2015 年间所有符合条件的特发性胰腺炎患者进行了遗传检测(PRSS1、CFTR、SPINK1 和 CTRC)。根据病历回顾,将患者分为以下几组:(1)有或无潜在慢性胰腺炎的复发性急性特发性胰腺炎(ARIP);(2)无 ARP 病史的特发性慢性胰腺炎(ICP);(3)年龄<35 岁的不明原因首发急性胰腺炎(AP);和(4)胰腺炎家族史。采用逻辑回归分析确定与致病性遗传变异相关的因素。
在 2010 年至 2015 年间评估的 197 例 ARIP 和/或 ICP 患者中,有 134 例接受了基因检测。在 64 例(47.8%)患者中发现了 88 种致病性遗传变异。在 ARIP、年龄<35 岁的不明原因首发 AP 和无 ARP 的 ICP 患者中,分别有 58%、63%和 27%的患者发现了致病性遗传变异。在调整分析中,ARIP(OR:18.12;95%CI:2.16-151.87;P=0.008)和年龄<35 岁的不明原因首发 AP(OR:2.46;95%CI:1.18-5.15;P=0.017),但不是 ICP,与致病性遗传变异独立相关。
致病性遗传变异最有可能在 ARIP 和年龄<35 岁的不明原因首发 AP 患者中被发现。对这些患者群体进行基因检测可能可以明确病因,并避免不必要的诊断性检查和操作。